E'lyse Murray

Inspired by “Phenomenal Woman,” #PhenomenalFriday honors women whose strength shapes history. Today, we spotlight Dr. Betty Shabazz — educator, civil rights advocate, and beloved friend of Dr. Maya Angelou. Bound by sisterhood, grace, and resilience, she carried justice forward with love. 🖤✨ #MayaAngelou #WomensHistoryMonth #BettyShabazz

Black/African Americans make up 43% of #lupus cases nationally & face worse outcomes. For treatments to effectively address this community's health needs, it’s crucial that Black/African Americans share their lupus experience w/patient-registries like RAY: buff.ly/D58I0aU

For many in the Black community, hair carries deep meaning. Experiencing hair loss from lupus can feel isolating, but you’re not alone. Learning how #lupus affects hair and scalp health can help you make informed care and styling choices. 👉 Learn more: buff.ly/P3K1xb8

We were proud to cheer on @OMG_itsizzyb and @NalyssaSmith as they played in support of #lupus warriors at the @AUProSports Causes Game! 💜🏀 Thank you both for standing with the Lupus Foundation of America during Causes Week and helping bring greater awareness to lupus.

@Rhiachnash CANT SLEEP

Join us for a fun night of Virtual Bingo with the LRA Walk Community! 🎉💻   📆 Thursday, December 11 🕢 7:30 pm EST   Let’s get together for the holidays and have some fun! Invite your team members, family, friends, and co-workers.    Tickets are $20 for admission, and include (2) Bingo boards. Additional Bingo boards are available for $5 each.   By participating in Bingo Night, you’ll be supporting the LRA and Walk With Us to Cure Lupus fundraising. 💜    For more information, visit bit.ly/47YVZ6T      Let the games begin!    #WalkWithUs #Lupus #LupusResearch

At last week's Breaking Through Gala, we honored @genentech as our 2025 Industry Partner Honoree.    Ashley Magargee, CEO, reflected on our long-standing collaboration — one rooted in advancing innovative science, accelerating clinical research, and ensuring the voices of people living with lupus guide the development of new therapies to bring hope to the entire community.    Our work together is a testament to the strength of steadfast partnership and what becomes possible when we unite behind a shared mission — working together every step of the way.    Thank you, Genentech, for driving progress forward with the Lupus Research Alliance!  #Lupus #LupusResearch #Partnership

The Lupus Research Alliance is seeking nominations for the 2026 Lupus Insight Prize recognizing and honoring an outstanding investigator with a documented record of creativity and innovation who has made a novel research discovery in scientific domains relevant to lupus between 2021 and 2025. To nominate a colleague from academia or industry, please review the Request for Nominations. Nominations due: December 1, 2025 🔗: bit.ly/46Nyn65

Happy #GivingTuesday! 🎉 Your gift to the Lupus Research Alliance will be matched up to $25,000, making your support go even further to fund groundbreaking lupus research and bring hope to patients worldwide. Why give to the Lupus Research Alliance today?    With federal funding cuts, private medical research is more crucial than ever—and the LRA is the largest private funder of lupus research, driving science forward where others cannot.     Please, make the Lupus Research Alliance your charity of choice today! LupusResearch.org  #LupusResearch #Lupus #GivingTuesday2025 #nonprofit #Donate #GiveBack #Charity

@halleberry What a beautiful honor and respect to your contribution to Art, Film and Equality as a Woman actor. Truly love poured into the decision of choosing @halleberry Epic.🔥💐💐💐🔥🔥🔥🔥💐

Best compliment ever ❤️🥰

Dr. Umar claims that Diddy is being used as a distraction to shift focus away from the 2024 presidential election: “They wanna distract you from the laws they are passing”

Today we celebrate #Juneteenth. On this day, it’s important to recognize the bias in healthcare that can prevent people of color, especially Black/African Americans, who are disproportionately impacted by lupus from receiving the best possible care. 🧵 1/2

A CMS proposal to “stack” rebates in Medicaid would harm medical innovation, providers, and patients who rely on access to lifesaving treatments. More from @BNyquist_MPH @infusioncenter on why @CMSgov must WITHDRAW the “stacking” policy. bit.ly/medicaid-stack… @CSROAdvocacy

@wiseconnector 88

@LupusResearch Great to see friends,sponsors walking, the opportunity supporting being a Volunteer, I am impacted with SLE Lupus and honored to be with you celebrating, helping the Lupus Research Alliance, #WalkwithLupus #ManyOneCan #ElyseMurraySpeaks

Rise and shine, NYC! We’re excited to see you at today’s Walk with Us to Cure Lupus at the Intrepid Museum! Join us and the #lupus community to celebrate your commitment to helping us find personalized treatments and ultimately a cure: bit.ly/NYC-Walk2023 Tag us: #ManyOneCan

@jamalhbryant Amen Amen reposting

@ChloeBailey Fiyah get it girl love the creativity the gift that was instilled in you🔥🔥🔥🔥🔥🔥🔥

get tix: chloebailey.net

this barbie’s going on tour 💖

@AngelaWinbush7 He works hard…. Beautiful

#BoyRuss (my rd Mgr)I got him on my selfie